(R)- and (S)-5-trimethylsilyl-2-cyclohexenone: a versatile chiral source for the synthesis of optically active cyclohexanone derivatives
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (46) , 5669-5672
- https://doi.org/10.1016/s0040-4039(00)96809-6
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Me3SiCl/HMPA accelerated conjugate addition of catalytic copper reagent. Stereoselective synthesis of enol silyl ether of aldehydeTetrahedron Letters, 1986
- Optical rotatory dispersion studies. 138. Synthesis and conformational analysis of .beta.-heteroatom-substituted cyclohexanonesThe Journal of Organic Chemistry, 1985
- The first stereoselective synthesis of (+)-nuciferol and (+)-nuciferalTetrahedron Letters, 1982
- Addition of aromatic thiols to conjugated cycloalkenones, catalyzed by chiral .beta.-hydroxy amines. A mechanistic study of homogeneous catalytic asymmetric synthesisJournal of the American Chemical Society, 1981
- Silicon-directed Baeyer-Villiger reactions. Stereospecific synthesis of olefinic acids and estersJournal of the American Chemical Society, 1980
- Silylation reductrice de derives monoaromatiques fonctionnelsJournal of Organometallic Chemistry, 1975
- Studies in sesquiterpenes—XXXVIITetrahedron, 1968